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Beneficial metabolic effects of PAHSAs depend on the gut microbiota in diet-induced obese mice but not in chow-fed mice.
Lee, Jennifer; Wellenstein, Kerry; Rahnavard, Ali; Nelson, Andrew T; Holter, Marlena M; Cummings, Bethany P; Yeliseyev, Vladimir; Castoldi, Angela; Clish, Clary B; Bry, Lynn; Siegel, Dionicio; Kahn, Barbara B.
Afiliação
  • Lee J; Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02215.
  • Wellenstein K; Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02215.
  • Rahnavard A; Department of Biostatistics and Bioinformatics, Milken Institute School of Public Health, George Washington University, Washington, DC 20052.
  • Nelson AT; Division of Pharmaceutical Chemistry, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, CA 92093.
  • Holter MM; Department of Biomedical Sciences, Cornell University College of Veterinary Medicine, Cornell University, Ithaca, NY 14850.
  • Cummings BP; Department of Surgery, School of Medicine, University of California, Davis, Sacramento, CA 95817.
  • Yeliseyev V; Department of Molecular Biosciences, School of Veterinary Medicine, University of California Davis School of Veterinary Medicine, Davis, CA 95616.
  • Castoldi A; Massachusetts Host-Microbiome Center, Department of Pathology, Brigham & Women's Hospital and Harvard Medical School, Boston, MA 02115.
  • Clish CB; Laboratory of Immunopathology Keizo Asami, Federal University of Pernambuco, Recife 50670-901, Brazil.
  • Bry L; Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, MA 02142.
  • Siegel D; Massachusetts Host-Microbiome Center, Department of Pathology, Brigham & Women's Hospital and Harvard Medical School, Boston, MA 02115.
  • Kahn BB; Division of Pharmaceutical Chemistry, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, CA 92093.
Proc Natl Acad Sci U S A ; 121(28): e2318691121, 2024 Jul 09.
Article em En | MEDLINE | ID: mdl-38968121
ABSTRACT
Dietary lipids play an essential role in regulating the function of the gut microbiota and gastrointestinal tract, and these luminal interactions contribute to mediating host metabolism. Palmitic Acid Hydroxy Stearic Acids (PAHSAs) are a family of lipids with antidiabetic and anti-inflammatory properties, but whether the gut microbiota contributes to their beneficial effects on host metabolism is unknown. Here, we report that treating chow-fed female and male germ-free (GF) mice with PAHSAs improves glucose tolerance, but these effects are lost upon high fat diet (HFD) feeding. However, transfer of feces from PAHSA-treated, but not vehicle-treated, chow-fed conventional mice increases insulin sensitivity in HFD-fed GF mice. Thus, the gut microbiota is necessary for, and can transmit, the insulin-sensitizing effects of PAHSAs in HFD-fed GF male mice. Analyses of the cecal metagenome and lipidome of PAHSA-treated mice identified multiple lipid species that associate with the gut commensal Bacteroides thetaiotaomicron (Bt) and with insulin sensitivity resulting from PAHSA treatment. Supplementing live, and to some degree, heat-killed Bt to HFD-fed female mice prevented weight gain, reduced adiposity, improved glucose tolerance, fortified the colonic mucus barrier and reduced systemic inflammation compared to HFD-fed controls. These effects were not observed in HFD-fed male mice. Furthermore, ovariectomy partially reversed the beneficial Bt effects on host metabolism, indicating a role for sex hormones in mediating the Bt probiotic effects. Altogether, these studies highlight the fact that PAHSAs can modulate the gut microbiota and that the microbiota is necessary for the beneficial metabolic effects of PAHSAs in HFD-fed mice.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Resistência à Insulina / Dieta Hiperlipídica / Microbioma Gastrointestinal / Obesidade Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Resistência à Insulina / Dieta Hiperlipídica / Microbioma Gastrointestinal / Obesidade Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article